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Drug ReportsErtapenem
Invanz(ertapenem)
Ertapenem, Invanz (ertapenem) is a small molecule pharmaceutical. Ertapenem was first approved as Invanz on 2001-11-21. It is used to treat abdominal abscess, bacterial infections, bacteroides infections, escherichia coli infections, and haemophilus infections amongst others in the USA. It has been approved in Europe to treat bacterial infections, bacterial pneumonia, community-acquired infections, gram-negative bacterial infections, and staphylococcal infections amongst others.
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Events Timeline
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FDA approval date
EMA approval date
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Study first post date
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Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
respiratory tract diseasesD012140
urogenital diseasesD000091642
skin and connective tissue diseasesD017437
signs and symptoms pathological conditionsD013568
Trade Name
FDA
EMA
Ertapenem, Invanz (discontinued: Ertapenem)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Ertapenem sodium
Tradename
Company
Number
Date
Products
INVANZMerck & CoN-021337 RX2001-11-21
1 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
ertapenamANDA2021-05-27
ertapenemANDA2024-11-06
ertapenem sodiumANDA2024-12-17
invanzNew Drug Application2024-02-15
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
pneumoniaEFO_0003106D011014—
urinary tract infectionsEFO_0003103D014552N39.0
bacterial infections—D001424A49
intraabdominal infections—D059413—
staphylococcal skin infectionsEFO_1001849D013207L00
escherichia coli infectionsEFO_1001318D004927B96.20
pelvic infection—D034161—
soft tissue infections—D018461—
streptococcal infectionsEFO_1001476D013290—
pyelonephritisEFO_1001141D011704N10-N16
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Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
J: Antiinfectives for systemic use
— J01: Antibacterials for systemic use
— J01D: Other beta-lactam antibacterials in atc
— J01DH: Carbapenems
— J01DH03: Ertapenem
HCPCS
Code
Description
J1335
Injection, ertapenem sodium, 500 mg
Clinical
Clinical Trials
89 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InfectionsD007239EFO_0000544——291113
Communicable diseasesD003141———291113
Intraabdominal infectionsD059413———121—4
Prostatic hyperplasiaD011470EFO_0000284N40———1—1
HyperplasiaD006965EFO_0000536————1—1
HypersensitivityD006967HP_0012393T78.40———1—1
Immediate hypersensitivityD006969—————1—1
Healthy volunteers/patients——————1—1
Chronic kidney failureD007676EFO_0003884N18.9———1—1
Continuous ambulatory peritoneal dialysisD010531—————1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Urinary tract infectionsD014552EFO_0003103N39.0—14—16
Surgical wound infectionD013530———13——3
PneumoniaD011014EFO_0003106——11——2
Diabetic footD017719EFO_1001459———2——2
Abdominal injuriesD000007———11——1
SepsisD018805HP_0100806A41.9——1——1
Focal infectionD005490————1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Soft tissue infectionsD018461———1———1
Bacterial pneumoniaD018410EFO_1001272J15.9—1———1
Pelvic infectionD034161———1———1
Pelvic inflammatory diseaseD000292EFO_1001388N70-N77—1———1
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameErtapenem
INNertapenem
Description
Ertapenem is meropenem in which the one of the two methyl groups attached to the amide nitrogen is replaced by hydrogen while the other is replaced by a 3-carboxyphenyl group. The sodium salt is used for the treatment of moderate to severe susceptible infections including intra-abdominal and acute gynaecological infections, pneumonia, and infections of the skin and of the urinary tract. It has a role as an antibacterial drug. It is a carbapenemcarboxylic acid and a pyrrolidinecarboxamide. It is a conjugate acid of an ertapenem(1-).
Classification
Small molecule
Drug classantibacterial antibiotics, carbapenem derivatives
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Structure (InChI/SMILES or Protein Sequence)
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(=O)Nc4cccc(C(=O)O)c4)C3)[C@H](C)[C@H]12
Identifiers
PDB—
CAS-ID153832-46-3
RxCUI—
ChEMBL IDCHEMBL1359
ChEBI ID404903
PubChem CID150610
DrugBankDB00303
UNII IDG32F6EID2H (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
Invanz – Merck & Co
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Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 11,462 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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5,317 adverse events reported
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